methocarbamol 1000 mg/1
methocarbamol · TABLET, FILM COATED · FH2 PHARMA LLC
No Recall History
Plain English
methocarbamol is a tablet, film coated containing methocarbamol at 1000 mg/1, taken oral. Manufactured by FH2 PHARMA LLC.
Key Facts
- Brand Name
- methocarbamol
- Generic Name
- methocarbamol
- NDC Code (Product)
72887-873- Manufacturer
- FH2 PHARMA LLC
- Strength
- 1000 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA212707
- Drug Class
- Muscle Relaxant [EPC]
- Marketing Start
- 08/30/2024
Recall History
No Recall HistoryFrequently Asked Questions
What is methocarbamol used for?
methocarbamol contains methocarbamol. It is a tablet, film coated taken oral. Consult your doctor for specific uses.
Is methocarbamol a controlled substance?
methocarbamol is not classified as a controlled substance by the DEA.
What is the generic name for methocarbamol?
The generic name for methocarbamol is methocarbamol. There are 11 other brand versions of methocarbamol.
What is the NDC code for methocarbamol 1000 mg/1?
The NDC (National Drug Code) for methocarbamol 1000 mg/1 is 72887-873, listed by FH2 PHARMA LLC.
Other Methocarbamol Brands
See all →- Methocarbamol500 mg/172865-233
- Methocarbamol750 mg/180425-0490
- Methocarbamol500 mg/187063-040
- Methocarbamol500 mg/115014-910
- Methocarbamol500 mg/150090-0182
- METHOCARBAMOL500 mg/161919-368
- Methocarbamol500 mg/163629-1123
- Methocarbamol500 mg/167046-0538
- Methocarbamol500 mg/168071-3636
- Methocarbamol500 mg/169306-500
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)